| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:98608416-98608690 | Common:1; Rare:112; Clinvar (benign):1 | ||||
| chr2:98615959-98616265 | Common:1; Rare:71 | ||||
| chr2:98616318-98616534 | Common:1; Rare:62 | ||||
| chr2:99154885-99155054 | Common:1; Rare:69; Clinvar (benign):2 | ||||
| chr2:99180848-99181244 | Common:2; Rare:128 | ||||
| chr2:99337308-99337588 | Rare:104 | ||||
| chr2:100007430-100007568 | Rare:36 | ||||
| chr2:100104669-100104949 | Common:2; Rare:65 | ||||
| chr2:100105361-100105512 | Rare:37 | ||||
| chr2:100417379-100417460 | Rare:22 | ||||
| chr2:101002186-101002324 | Rare:52 | ||||
| chr2:101252685-101252971 | Common:4; Rare:95 | ||||
| chr2:101262469-101262573 | Common:1; Rare:29 | ||||
| chr2:101286741-101286777 | Rare:3 | ||||
| chr2:101474665-101474829 | Common:1; Rare:28 |